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Lectin BS‐I attenuated the binding of sGRP78 and p85. (A)Western blot detected the expression of GRP78 in surface and whole cells. (B) The alteration of intracellular localization of GRP78 treated by BS‐I with microscopy, bar = 50 μm. (C) Co‐immunoprecipitation of GRP78 and P85, using membrane protein from MHCC97L cells treated with 1 μg/ml BS‐I or incorporation with 25 mM Gal or GalNAc.
